Support
All our support activities provide a vital lifeline to LMBBS families, several of whom have more than one affected child.
The words of one of our Scottish members who described the discovery of our pamphlet, The LMBBS Child at School,
'Like Striking Gold'
when receiving her daughter's distressing diagnosis, help to illustrate the value of our work.
A mother of a 29 year old son with LMBBS said it felt like
'Winning The Lottery'
when she received Introducing LMBBS, never before having seen the condition so clearly explained.
The Laurence-Moon-Bardet-Biedl Society is a dynamic forum of people with LMBBS, their families, carers and professionals involved in the care and management of those with LMBBS.
All members of the Committee are volunteers.
Click on the links to the right, and see how you can help support LMBBS.
Other Pages in this section...
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